DK151803C - METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF - Google Patents
METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOFInfo
- Publication number
- DK151803C DK151803C DK400679A DK400679A DK151803C DK 151803 C DK151803 C DK 151803C DK 400679 A DK400679 A DK 400679A DK 400679 A DK400679 A DK 400679A DK 151803 C DK151803 C DK 151803C
- Authority
- DK
- Denmark
- Prior art keywords
- formula
- lower alkyl
- hydrogen
- acceptable salts
- pyrrol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
- C07D237/34—Phthalazines with nitrogen atoms directly attached to carbon atoms of the nitrogen-containing ring, e.g. hydrazine radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/20—Nitrogen atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyrrole Compounds (AREA)
Abstract
New N-pyrrolyl-3-pyridazine-amines having a further aminic substituent in the 6 position of the formula (I), <CHEM> wherein R, R1, R2 and R3 are hydrogen or lower alkyl, R4 is e.g. hydrogen or lower alkyl, R5 and R6 are e.g. lower alkyl or taken together with the adjacent nitrogen atom represent a saturated 5 - 6 membered heterocyclic ring which may contain a further heteroatom, R7 and R8 represent hydrogen or, taken together, a 1,3-butadienylene radical forming a benzo system fused with the pyridazine ring, for example N-2,5-dimethyl-1H-pyrrol-1-yl)- 6-morpholino-3-pyridazineamine or N-(2,5-dimethyl-1H-pyrrol- 1-yl)-4-(4-hydroxypiperidino)-1-phthalazineamine, and their pharmaceutically acceptable salts are made e.g. by contacting a hydrazino derivate of the formula (II), wherein the substituents have the same meaning as above or an acid addition salt thereof with a dicarbonyl compound of the formula (III), wherein the substituents have the same meaning as above, or a functional derivative thereof in the presence of an acid catalyst at a temperature between 15 DEG C and 120 DEG C. The new compounds can be used as antihypertensive agents.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7838898 | 1978-10-02 | ||
GB7838898 | 1978-10-02 |
Publications (3)
Publication Number | Publication Date |
---|---|
DK400679A DK400679A (en) | 1980-04-03 |
DK151803B DK151803B (en) | 1988-01-04 |
DK151803C true DK151803C (en) | 1988-06-13 |
Family
ID=10500040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK400679A DK151803C (en) | 1978-10-02 | 1979-09-25 | METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF |
Country Status (15)
Country | Link |
---|---|
EP (1) | EP0009655B1 (en) |
JP (1) | JPS5569577A (en) |
AT (1) | ATE3294T1 (en) |
AU (1) | AU529482B2 (en) |
CA (1) | CA1144165A (en) |
DE (1) | DE2965377D1 (en) |
DK (1) | DK151803C (en) |
ES (1) | ES484616A1 (en) |
FI (1) | FI65998C (en) |
GR (1) | GR69856B (en) |
IE (1) | IE49017B1 (en) |
IL (1) | IL58256A (en) |
NO (1) | NO151620C (en) |
YU (1) | YU41886B (en) |
ZA (1) | ZA794923B (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1150070B (en) * | 1980-12-22 | 1986-12-10 | Lepetit Spa | PROCEDURE FOR PREPARING N-PYROLIPYRIDAZINAMINIC DERIVATIVES |
US5254622A (en) * | 1988-12-09 | 1993-10-19 | Asahi Kasei Kogyo Kabushiki Kaisha | ABS resin compositions and molded articles thereof having improved coating performances |
JP4831577B2 (en) * | 2003-07-30 | 2011-12-07 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | Pyridazine derivatives and uses as therapeutic agents |
TW200626154A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
BRPI0515478A (en) | 2004-09-20 | 2008-07-22 | Xenon Pharmaceuticals Inc | heterocyclic derivatives and their use as mediators of stearoyl coa desaturase |
AU2005329423A1 (en) | 2004-09-20 | 2006-09-28 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
TW200626155A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
WO2006034279A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
CN101083982A (en) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-coa desaturase enzymes |
CN101084207A (en) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
BRPI0611187A2 (en) | 2005-06-03 | 2010-08-24 | Xenon Pharmaceuticals Inc | amino thiazide derivatives as inhibitors of human stearoyl coa desaturase |
USD916552S1 (en) * | 2019-07-26 | 2021-04-20 | Spectrum Diversified Designs, Llc | Trivet |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1168334A (en) * | 1967-01-25 | 1969-10-22 | Lepetit Spa | New Pharmacologically Active Pyridazines |
GB1378102A (en) * | 1972-03-14 | 1974-12-18 | Lepetit Spa | Antihypertensive compositions |
GB1408362A (en) * | 1973-05-25 | 1975-10-01 | Lepetit Spa | 2-pyrrol-1-yl amino 4,5-dihydro-1-h-imidazole derivatives |
AU477837B2 (en) * | 1973-05-30 | 1974-12-05 | I. S. F. Sp. A | New anti-hypertensive compounds having a high therapeutic index and a long-term hypotensive effect |
ES431009A1 (en) * | 1974-05-09 | 1976-10-16 | Isf Spa | Process for the preparation of benzylidene derivatives |
-
1979
- 1979-09-07 AT AT79103326T patent/ATE3294T1/en active
- 1979-09-07 DE DE7979103326T patent/DE2965377D1/en not_active Expired
- 1979-09-07 EP EP79103326A patent/EP0009655B1/en not_active Expired
- 1979-09-12 FI FI792832A patent/FI65998C/en not_active IP Right Cessation
- 1979-09-14 AU AU50866/79A patent/AU529482B2/en not_active Ceased
- 1979-09-17 IL IL58256A patent/IL58256A/en unknown
- 1979-09-17 ZA ZA00794923A patent/ZA794923B/en unknown
- 1979-09-24 GR GR60097A patent/GR69856B/el unknown
- 1979-09-25 DK DK400679A patent/DK151803C/en not_active IP Right Cessation
- 1979-09-28 YU YU2374/79A patent/YU41886B/en unknown
- 1979-10-01 ES ES484616A patent/ES484616A1/en not_active Expired
- 1979-10-01 IE IE1866/79A patent/IE49017B1/en not_active IP Right Cessation
- 1979-10-01 NO NO793151A patent/NO151620C/en unknown
- 1979-10-02 JP JP12647779A patent/JPS5569577A/en active Granted
- 1979-10-02 CA CA000336843A patent/CA1144165A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FI792832A (en) | 1980-04-03 |
DK151803B (en) | 1988-01-04 |
EP0009655B1 (en) | 1983-05-11 |
GR69856B (en) | 1982-07-19 |
IL58256A (en) | 1984-02-29 |
JPS5569577A (en) | 1980-05-26 |
ZA794923B (en) | 1980-09-24 |
NO793151L (en) | 1980-04-08 |
ATE3294T1 (en) | 1983-05-15 |
EP0009655A1 (en) | 1980-04-16 |
IE791866L (en) | 1980-04-02 |
AU5086679A (en) | 1980-04-17 |
IE49017B1 (en) | 1985-07-10 |
FI65998B (en) | 1984-04-30 |
JPH0321553B2 (en) | 1991-03-22 |
AU529482B2 (en) | 1983-06-09 |
DK400679A (en) | 1980-04-03 |
DE2965377D1 (en) | 1983-06-16 |
NO151620C (en) | 1985-05-08 |
CA1144165A (en) | 1983-04-05 |
YU41886B (en) | 1988-02-29 |
ES484616A1 (en) | 1980-05-16 |
YU237479A (en) | 1983-02-28 |
IL58256A0 (en) | 1979-12-30 |
NO151620B (en) | 1985-01-28 |
FI65998C (en) | 1984-08-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PBP | Patent lapsed |